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Tuesday, May 3rd, 2011

Immunetics Awarded $2.4 Million NIH Grant for Clinical Trials of New Blood Test for Chagas’ Disease

immunetics-release-logoBOSTON – May 3, 2011Immunetics, Inc. today announced it has been awarded a $2.4 million, 3-year Phase II SBIR grant by the National Institute of Allergy and Infectious Diseases, a division of the National Institutes of Health (NIH), to support clinical trials of the company’s new confirmatory test for Chagas’ disease, a serious and potentially fatal parasitic infection.

Chagas’ disease is endemic in large parts of Latin America, where it affects up to 11 million people, and has emerged in the U.S., where more than 300,000 people are infected, according to the Centers for Disease Control and Prevention. The disease is difficult to diagnose, and is often silent for years before clinical symptoms appear. During this time, carriers can pass on the parasite through blood donations and infect transfusion recipients.

Existing screening tests that detect antibodies to the parasite are frequently inaccurate. A complex method called radioimmunoprecipitation (RIPA) is sometimes used to confirm screening test results, but is beyond the reach of most laboratories. There are no FDA-approved confirmatory test methods.

Immunetics’ test, called an immunoblot, detects antibodies to the parasite and is based on the same technology used in confirmatory tests for HIV and several other bloodborne infections. Data presented by Immunetics at meetings in 2010 of the American Association of Blood Banks and the American Society of Tropical Medicine and Hygiene showed the immunoblot test to be as accurate as RIPA in preliminary studies, said Dr. Andrew Levin, president and scientific director, Immunetics.

“The new NIH grant will enable Immunetics to undertake a full-scale clinical trial to obtain data to submit to the FDA for approval of the immunoblot as a confirmatory test. Immunetics will undertake the studies with collaborators at Blood Systems Research Institute, the American Red Cross, and the Centers for Disease Control and Prevention,” Levin said.

“This grant award gives us the opportunity to take our Chagas’ immunoblot test through the clinical studies needed to establish its validity as a confirmatory test. We are very grateful for NIH support for this project, which will allow us to bring forward a practical solution to one part of the growing public health and blood safety problem that Chagas’ disease presents in the U.S. and Latin America,” he said.

About Immunetics, Inc.

Immunetics Inc., (http://www.immunetics.com) offers state-of-the-art assay technology for infectious disease diagnosis and pathogen detection, and for over 10 years has been a leading innovator of tests for bacterial, viral, and parasitic diseases. The company produces and markets a range of infectious disease assay kits and instruments. Its mission is better, cost-efficient care through more accurate diagnosis. Immunetics is headquartered in Boston, Mass. Follow Immunetics on Twitter at http://twitter.com/immunetics.

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Press Contact: Don Goncalves, Tiziani Whitmyre, 781-793-9380, dgoncalves@tizinc.com


Wednesday, April 6th, 2011

Seminar to Help Manufacturers Accelerate the Process of Bringing Reusable Medical Devices to Market

AGAWAM, Mass. – Medical product manufacturers can learn how to accelerate the process of bringing their reusable devices to market in a day-long seminar on May 3, 2011, in Dedham, Massachusetts.

Titled “Bringing Your Reusable Device To Market: Just Because Your Device Lasts Forever Doesn’t Mean The Process of Bringing It To Market Has To,” the seminar will provide an extensive look at the process of introducing such products and help manufacturers answer critical questions such as: “What is required?”; “How much will it cost?”; and “How long will it take?”

The seminar will cover the product introduction process from manufacture of the sterilization tray to the testing that’s required for regulator submittal. Presentations will include:

  • Flushing It Out: New Analytical Methods of Testing on Protein, Hemoglobin, and Carbohydrate
  • Don’t Get Stuck in a Groove: Cleaning Validations Using Microbial Methods
  • What is the Good in Good Laboratory Practices (GLP): Understanding the Process
  • Packaging Your Idea Into Reality: A Look at the Process of Tray Manufacturing
  • One Cycle, Two Cycle, Three Cycle, More?: Sterilization of Your Reusable Devices

The event will run from 8:30 a.m. to 3:30 p.m., with registration and a complimentary continental breakfast starting at 8 a.m. The seminar will be held on Tuesday, May 3, 2011, at the MIT Endicott House, 80 Haven Street, Dedham, Massachusetts. The cost is $149 per person and it includes breakfast, lunch, and workshop handouts.

The seminar is sponsored by Microtest Laboratories, a leader in testing services and contract manufacturing for the medical device, pharmaceutical, and biotechnology industries.

To register, contact Julie Adamski at 413-786-1680, toll-free at 800-631-1680, or at jadamski@microtestlabs.com.

About Microtest Laboratories

Microtest Laboratories is a leader in testing services and contract manufacturing for the medical device, pharmaceutical, and biotechnology industries. Based in Agawam, Massachusetts, USA, the company provides expertise and flexible processes that enhance product safety and security, accelerate time to market, and minimize supply chain disruption. For more information, visit http://www.microtestlabs.com or call 1-413-786-1680 or toll-free 1-800-631-1680. Follow Microtest Laboratories on Twitter @MicrotestLabs at http://twitter.com/MicrotestLabs.

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Press contact: Don Goncalves, 1-781-793-9380, dgoncalves@tizinc.com


Wednesday, March 30th, 2011

Immunetics Featured at Boston Startup America Event

immunectics1BOSTON, MASSACHUSETTS, March 30, 2011 - “Immunetics came to the South Boston Innovation District after recognizing that an attractive business location with talented people, reasonable facility costs, and access to capital would be a great place to achieve their next stage of growth,” Mayor Menino said. “Now, the city’s partnership with Immunetics has generated benefits that exceeded all of our expectations. Together, we’ve created jobs, won millions of dollars in grants and contracts, and most importantly, achieved medical advances that will help millions of people overcome life-threatening diseases.”

Immunetics President and Chief Executive Officer Dr. Andrew Levin said LifeTech Boston, the Mayor’s program that supports the life sciences industry in the city and is administered through the Boston Redevelopment Authority, helped locate a facility that could support the company’s growth objectives, plus secure a loan to finance its build-out.

“Since then, we have almost tripled the size of our workforce, won over $22 million in grants and contracts, and developed better diagnostics for diseases such as HIV, Lyme disease, and other serious infections that threaten our blood supply,” said Dr. Levin. “Our move to the Innovation District has been the key to Immunetics’ growth and success over the past 7 years.”

The Startup America initiative’s goal is to increase opportunities for entrepreneurs by expanding access to capital, developing education and mentorship programs, and improving collaboration between startup and established companies.

About Immunetics
Immunetics (http://www.immunetics.com) offers state-of-the-art assay technology for infectious disease diagnosis and pathogen detection. For over 10 years, the company has been a leading innovator of tests for bacterial, viral, and parasitic diseases. Immunetics produces and markets a range of infectious disease assay kits and instruments. Its mission is better, cost-efficient care through more accurate diagnosis.


Tuesday, January 18th, 2011

University of Alabama at Birmingham Brain Cell Injury Study Utilizes InQ Cell Research System

Huntsville, Ala. – January 18, 2011 — InQ Biosciences, a provider of innovative technologies for cell growth and research, today announced that a pre-commercial version of its InQ Cell Research System is being utilized in a University of Alabama at Birmingham (UAB) study evaluating the effects of secondary injury components on brain cells. The InQ system integrates a dynamically controlled sample environment with advanced live cell imaging and real-time data collection.


The study is being conducted by Candace L. Floyd, Ph.D., assistant professor in UAB’s Department of Physical Medicine and Rehabilitation and its Center for Glial Biology in Medicine and a member of the InQ Biosciences Scientific Advisory Board.


At UAB, Dr. Floyd leads a translational research laboratory that researches novel treatments for traumatic brain and traumatic spinal cord injury. The study could ultimately provide a foundation for screening therapeutics to benefit individuals suffering a brain injury or stroke.


“We know that different cells in the brain – astrocytes, neurons, microglia, and others – respond differentially to injury,” said Dr. Floyd. “But we’re not sure how they interact or what causes a temporal series of events. If a person with a brain injury goes into hyperglycemia or hypoglycemia, their outcome is usually significantly worse. But no one knows why,” she said.


“With the InQ system’s real-time microscope and very specific control of environmental conditions, we can replicate these injury components and evaluate individually in temporal course the response of each cell type,” said Dr. Floyd. “We will grow brain cells either as a mixture of cells-neurons, astrocytes, microglia together-or as an individual population. We’ll expose these cells to a hypoxic insult, simulating what happens in a stroke, or a hyperglycemic insult, which is a complication after a traumatic brain injury, and then evaluate the effects in real time,” she said.


Dr. Floyd said the InQ system provides “a very precise control of environmental conditions that is not currently available in the market. Researchers can control temperature, gas, and media, with absolute control while using the microscope system to monitor the cell response in real time. This technology has not previously existed prior to the development of this system,” she noted.


“Without InQ technology, the same degrees of temporal resolution and experimental control would not be possible,” Dr. Floyd said. “Instead, the cells would be grown in a Petri dish, the media would be changed to create the required conditions, and then the cells would be moved to a microscope for monitoring. There would be gaps of information between the manipulations and no real-time observation. The InQ system enables a researcher to fill in those gaps and achieve distinct temporal resolution of the sequence of events,” she explained.


About the InQ system


The InQ system combines a dynamic software-controlled sample environment with powerful imaging and real-time data collection. The system tightly controls environmental parameters with correlated sample feedback. The benchtop system automates the cell culture process by enclosing the cells in a sealed, sterile removable cartridge that slides into the instrument. An onboard computer precisely controls the mix and flow of nutritive media and gasses and regulates the temperature. A built-in high-resolution microscope and camera record the assay at scheduled intervals, and can send the images to the researcher anywhere in the world via the Internet and smart phone. Adjustments to the experiment can also be made remotely. The InQ system fits easily into research workflows and integrates with most laboratory information management systems.


About InQ Biosciences


InQ Biosciences is a provider of innovative technologies for cell growth and research. The company’s InQ Cell Research system will empower scientists to unlock novel and more powerful approaches to cell-based discovery. The firm was founded in 2007 with technology originating from the University of Alabama in Huntsville. Series B financing was completed in May 2010 and commercial launch of its InQ system is scheduled for the first quarter of 2011. For more information, visit www.inqbio.com. Follow InQ Biosciences on Twitter at @InQbio (http://twitter.com/InQbio).


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Thursday, January 6th, 2011

Century Park Capital Partners Announces the Recapitalization of Cirtec Medical Systems, LLC

January 6, 2011, LOS ANGELES – Century Park Capital Partners is pleased to announce that it led the recapitalization of Cirtec Medical Systems LLC (“Cirtec”) along with Charter Oak Equity and the company’s founders. Cirtec is a leading provider of client focused, comprehensive medical product design, engineering and manufacturing solutions. Cirtec provides its customers with highly technical solutions, utilizing its expertise in minimally invasive systems, active and passive implants, and medical electronics. Cirtec was formed in 2009 from the merger of Circle Medical Devices and Texcel Medical. The company operates out of locations in Los Gatos, California and East Longmeadow, Massachusetts.

“We chose to partner with Century Park because of their philosophy of collaborating with management and their track record of successfully helping businesses grow,” stated Barry Smith, CEO of Cirtec. “Century Park’s leadership and access to resources will allow us to maintain our industry leading position in the outsourced medical device design and manufacturing industry as we take our business to the next level.”

Larry Derose, one of the founders of the company said, “This partnership with Century Park is the next step in our company’s evolution. By coupling our success in the market with Century Park’s proven experience helping businesses of our size grow, we have become exceptionally well positioned to capture the tremendous opportunities that exist in our marketplace.”

Century Park Capital Partners has experienced success in the medical device arena through prior investments in the medical contract manufacturing sector.

Chip Roellig, a Managing Partner of Century Park, stated, “We are very enthusiastic about our new partnership with Cirtec. Cirtec’s reputation as the market leader and its customer relationships with major medical device OEMs in the neurostimulation and cardiovascular markets set the company apart from other medical device design and manufacturing firms. Cirtec is especially attractive because they offer their customers a range of highly technical capabilities that improve device design and reduce time to market for new devices, while offering a superior economic value proposition. Furthermore, Cirtec is well positioned to take advantage of the trend in increased outsourcing of medical device design and manufacturing. As neurostimulation and cardiovascular devices evolve and gain further acceptance, Cirtec is primed for growth.”

Terms of the transaction were not disclosed. The investment by Century Park was made from its latest fund, Century Park Capital Partners II, L.P.

About Cirtec Medical Systems

Cirtec Medical Systems, through its partnerships with its customers, has become a leading single-source provider of comprehensive medical product design and manufacturing solutions from concept through high-volume finished goods across all therapeutic categories. Its technically-driven, 130-person team has particular expertise in minimally invasive systems, active and passive implants, and medical electronics. Cirtec Medical Systems is ISO-13485 (2003) and FDA certified and maintains locations in Los Gatos, California and East Longmeadow, Massachusetts. For more information about Cirtec, please visit www.cirtecmed.com.

About Century Park Capital Partners

Century Park Capital Partners is a Los Angeles-based private equity firm that partners with owner/managers to build successful companies. The firm specializes in facilitating owner liquidity and business expansion by providing equity for recapitalizations, buyouts, growth financings, and acquisitions. More information on Century Park Capital Partners can be found at www.centuryparkcapital.com.

About Charter Oak Equity

Charter Oak Equity is a Westport, CT based private equity firm. Charter Oak Equity focuses on niche manufacturing, packaging, medical products & services, specialty chemicals, consumer products and financial services companies ranging in size from $5 million to $150 million in enterprise value.  More information on Charter Oak Equity can be found at www.charteroak-equity.com.

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Public Relations contact, Boston:  Don Goncalves, dgoncalves@tizinc.com, 781-793-9380, for Tiziani Whitmyre Inc., http://www.tizinc.com/public-relations


Monday, December 13th, 2010

InQ Biosciences to Commercialize Cell Research System in First Quarter 2011

HUNTSVILLE, ALABAMA, December 13, 2010 — InQ Biosciences, a provider of innovative technologies for cell growth and research, announced today it will commercially release its InQ Cell Research System during the first quarter of 2011. InQ is the first fully integrated system that creates a high-fidelity in vitro environment for studying stem cells –as well as nerve, brain or any other cells that can be grown in a Petri dish for disease research.

In an announcement at the 2010 Annual Meeting of the American Society for Cell Biology, the company said it will begin commercial production of the InQ system in early 2011 and will accept orders beginning immediately.

“This milestone represents the first cell research application of our InQ technology that promises critical new discoveries in stem cell biology and in the causes and treatment of neurological disorders, cancer, and cardiovascular diseases,” said Aaron Hammons, president and chief technology officer, InQ Biosciences. “By integrating a dynamically controlled sample environment, advanced imaging, and real-time data collection, the InQ system empowers scientists with an exciting new tool that accelerates diagnostic and therapeutic discoveries.”

Hammons said InQ technology is the first to offer the following advantages:

· High-fidelity simulation of the human body environment, including circadian temperature rhythms and numerous disease states

· Precise, automated management of temperature, gas levels, media perfusion, pressure, and waste removal

· Automated onboard microscopy for real-time monitoring and analysis

· Unprecedented local/remote access and control

“Now a researcher can simulate hundreds of disease states and conduct event-based analyses while improving laboratory productivity,” he said.

Floyd Presents First InQ Data

Dr.Candace Floyd, assistant professor, Department of Physical Medicine and Rehabilitation, University of Alabama at Birmingham, and member of InQ Biosciences Scientific Advisory Board, said her initial experience testing the InQ system showed promising results. “We were able to grow, under tight conditions, various types of cells whose quality is equal to or better than those cultured in a Petri dish,” said Dr. Floyd. “We have confirmed the growth of exceptionally well formed astrocytes and neurons from the brain as well as cardiac myocytes.

“With InQ technology, you are able to push the envelope of discovery by having much more precise control over your experiments and a real-time readout of the variables you choose for your cellular biology,” Dr. Floyd said.

Dr. Todd McDevitt, associate professor, Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, and member of InQ Biosciences’ Scientific Advisory Board, said the system will significantly enhance stem cell research.

“With InQ, you can perform an experiment where you keep conditions constant, replenish them at high frequency, or even make very rapid changes in the culture environment,” said Dr. McDevitt. “Then you can map the results back to those conditions and get to causality much better than the correlative types of research initially done in cell biology. I think this technology will expedite the entire stem cell research process because scientists can now create fancy constructs,” he said.

The InQ system automates the cell culture process by enclosing the cells in a sealed, sterile removable cartridge that slides into the instrument. An onboard computer precisely controls the mix and flow of nutritive media and gasses and regulates the temperature. A built-in high-resolution microscope and camera record the assay and can send the images to the researcher anywhere in the world via the Internet and smart phone. The InQ System fits easily into research workflows and integrates with most laboratory information management systems.

For more information on the InQ System, contact info@inqbio.com or 866-735-9684, or visit http://www.inqbio.com.

About InQ Biosciences

InQ Biosciences is a provider of innovative technologies for cell growth and research. The company’s InQ Cell Research System will empower scientists to unlock novel and more powerful approaches to cell-based discovery. The firm was founded in 2007 with technology originating from the University of Alabama in Huntsville. Series B financing was completed in May 2010 and commercial launch of its InQ system is scheduled for the first quarter of 2011. For more information, visit http://www.inqbio.com. Follow InQ Biosciences on Twitter at http://twitter.com/InQbio.

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Public Relations contact, Boston:  Don Goncalves, dgoncalves@tizinc.com, 781-793-9380, for Tiziani Whitmyre Inc., http://www.tizinc.com/public-relations


Wednesday, December 8th, 2010

New White Paper Examines Clinical Trial Material Production & Testing: What Your Contract Manufacturing Organization is Not Telling You

AGAWAM, MASS. – For pharmaceutical manufacturers, delays in starting a clinical trial program due to issues involving the manufacture of clinical trial material (CTM) and the associated fill/finish and release work can make even the most dogged project managers wince in pain. A new, free white paper recommends a proven process of evaluating a cGMP contract manufacturing organization (CMO) to deliver all the required processes needed to release CTM for clinical trial use.

The new white paper, “Clinical Trial Material Production and Testing: Is Your CMO Providing Everything You Need,” explores what pharmaceutical manufacturers must require from a CMO in terms of capabilities and expertise and the critical roles that the contractor must be able to assume in the clinical trial material manufacturing process.

The white paper is available for download from: http://www.microtestlabs.com/clinical-trial-material-production-testing-paper/.

“In order to keep clinical protocols on time and on budget in the CTM manufacturing process, it’s critical that the selected CMO has comprehensive capabilities that are both in-house and readily available,” notes Alexander Mello, author of the white paper and Director of Project Management, Manufacturing, for Microtest Laboratories, a leader in contract manufacturing, aseptic processing and full service pharmaceutical testing.

“Contracting with a CMO without complete in-house expertise will add unnecessary time to the CTM process. In these cases, performing a GMP audit of the CMO, plus all of the other companies (formulators, laboratories, labelers, etc.) that the CMO uses in the supply chain, will add significantly to the overall cost and time for the technical transfer of the product,” he explains.

The new white paper illustrates how the proper selection of a CMO can help meet product schedules and minimize potential restart activities. The paper reviews the roles that the CMO must be able to play in CTM process, from first steps through the completion, and details the key areas of Raw Materials, Formulation, and Final Drug Product (FDP).

The white paper also discusses how a fully-capable CMO will have the ability to perform all the required processes in CTM – including excipient and API release for GMP manufacture, formulation, in-process testing, environmental monitoring, filter integrity testing, and final release testing.

To download the new, free white paper, “Clinical Trial Material Production and Testing: Is Your CMO Providing Everything You Need,” visit http://www.microtestlabs.com/clinical-trial-material-production-testing-paper/.

Mello, the author of the white paper, is Director of Project Management, Manufacturing, for Microtest Laboratories. Mello’s 15 years of experience span Aseptic Fill/Finish, Microbiology, Method Transfer, Stability of Drug Product, Medical Devices/Combo Devices, and Sterilization Sciences. He holds a graduate degree in Biological Sciences and is a Specialist Microbiologist (NRM).

Follow Microtest Labs on Twitter @MicrotestLabs at http://twitter.com/MicrotestLabs.

About Microtest

Microtest is a leader in testing services and contract manufacturing for the medical device, pharmaceutical, and biotechnology industries. Based in Agawam, Massachusetts, U.S.A., the company’s expertise and flexible processes enhance product safety and security, accelerate time to market, and minimize supply chain disruption. For more information, visit http://www.microtestlabs.com or call 1-413-786-1680 or toll-free 1-800-631-1680.

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Public Relations contact, Boston:  Don Goncalves, dgoncalves@tizinc.com, 781-793-9380, for Tiziani Whitmyre Inc., http://www.tizinc.com/public-relations


Wednesday, December 1st, 2010

InQ Biosciences to Introduce First Integrated Cell Research System at ASCB Annual Meeting

Huntsville, Ala. – December 1, 2010– InQ Biosciences, a provider of innovative technologies for cell growth and research, will introduce its InQ™ Cell Research System – the first fully integrated cell growth and cell analysis system that combines a dynamically controlled sample environment with powerful imaging and real-time data collection – at the American Society for Cell Biology’s (ASCB) 2010 Annual Meeting in Philadelphia.

In addition, Candace L. Floyd, Ph.D., assistant professor in the Department of Physical Medicine and Rehabilitation at the University of Alabama at Birmingham and its Center for Glial Biology in Medicine, will discuss her experience testing the efficacy of the InQ system and its ability to grow various types of brain cells of equal or better quality than those grown in a Petri dish.

Dr. Floyd has already confirmed the growth of “exceptionally well formed” astrocytes and neurons as well as cardiac myocytes using the InQ system and is continuing to test the development of other cell types used in medical research. She is a member of the InQ Biosciences Scientific Advisory Board.

“The InQ system accurately models the conditions found in the human body that are essential for healthy cell growth and analysis. It is an essential tool for researchers studying the effects of disease and environment on human and animal cells,” said Aaron Hammons, InQ Biosciences president and chief technology officer.

“The InQ system’s exclusive ability to control environmental parameters with correlated real-time sample feedback empowers researchers with novel and efficient approaches to discovery,” he said.

InQ technology is the first to offer:

  • The ability to create a high-fidelity simulation of the human body environment
  • Precise management of temperature, gas levels, media perfusion, and pressure for extended cell growth
  • Advanced automated onboard microscopy with remote monitoring for superior cell analysis
  • Unprecedented reproducibility and standardization
  • Greater visualization and exceptional data quality

For more information, visit InQ Biosciences in booth #849 at the ASCB 2010 Annual Meeting, Dec. 11-15 in Philadelphia, or visit the company’s website at http://www.inqbio.com. Follow InQ bio on Twitter at @InQBio or http://twitter.com/inqbio.

About InQ Biosciences

InQ Biosciences is a provider of innovative technologies for cell growth and research. The company’s InQ Cell Research System will empower scientists to unlock novel and more powerful approaches to cell-based discovery. The firm was founded in 2007 with technology originating from the University of Alabama in Huntsville. Series B financing was completed in May 2010 and commercial launch of its InQ system is scheduled for the first quarter of 2011. For more information, visit www.inqbio.com. Follow InQ Biosciences on Twitter at @InQbio (http://twitter.com/InQbio).

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Public Relations contact, Boston:  Don Goncalves, dgoncalves@tizinc.com, 781-793-9380, for Tiziani Whitmyre Inc., http://www.tizinc.com/public-relations


Monday, November 22nd, 2010

InQ Biosciences Announces New Board Members

Huntsville, Ala. – InQ Biosciences Corporation, a provider of innovative technologies for cell growth and research, announced that Michael Chambers and John R. Cooper have been appointed to the board of directors.

“Michael and John bring successful leadership and deep experience in life science and technology to the Board. We look forward to applying their spirit of innovation and success to the growth of InQ Biosciences,” said Dick Reeves, chairman and chief executive officer, InQ Biosciences.

Michael Chambers, Ph.D. is President and CEO of Swift Biotechnology, an emerging company targeting development of cancer diagnostics. He actively invests in early-stage high-growth companies and serves on the board of ProUroCare, a publicly traded company. Previously, Chambers helped establish InnoRx Pharmaceuticals in 1999, a company specializing in development of drugs and drug delivery systems for ocular disease. He served as president and CEO of InnoRx until negotiating its sale and merger into SurModics.

John Cooper is the retired chairman and CEO of publicly traded Avocent Corporation. From 2002 until 2008, he led Avocent through a period of rapid growth to become one of the largest companies in local and remote IT infrastructure management. From 1996 to 2001, Mr. Cooper was chief financial officer and senior vice president for finance and administration, of publicly traded ADTRAN, Inc., a leading global provider of networking and telecommunications solutions with revenues of $300 million.

InQ Biosciences provides the InQTM Cell Research System, the first fully integrated system that creates an in vivo-like environment for studying sensitive nerve, brain, and other human cells for disease research. It is the only cell research instrument that combines a dynamic software-controlled sample environment with powerful imaging and real-time data collection. These unique capabilities enable researchers to achieve unprecedented cell culture control, viability, and visibility that was previously unattainable.

About InQ Biosciences

InQ Biosciences is a provider of innovative technologies for cell growth and research. The company’s InQ Cell Research System will empower scientists to unlock novel and more powerful approaches to cell-based discovery. The firm was founded in 2007 with technology originating from the University of Alabama in Huntsville. Series B financing was completed in May 2010 and commercial launch of its InQ system is scheduled for the fourth quarter of 2010. For more information, visit http://www.inqbio.com. Follow InQ Biosciences on Twitter at @InQbio (http://twitter.com/InQbio).

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Public Relations contact, Boston:  Don Goncalves, dgoncalves@tizinc.com, 781-793-9380, for Tiziani Whitmyre Inc., http://www.tizinc.com/public-relations


Tuesday, November 16th, 2010

New White Paper: Having a Solid Package Validation Program Can Prevent Failure of Combination Products

AGAWAM, MASS. – November 16, 2010 – A new white paper urges medical device and combination product manufacturers to employ a solid package validation program as a means of preventing the failure of combination products.

“FDA concerns regarding terminally sterilized medical products are based on years of data that implicate failures in primary packaging. Approximately 47% of failures occur due to inadequate package validation programs,” said Steven Richter, Ph.D., founder, president and chief scientific officer of Microtest Laboratories in Agawam, Mass.

Richter is author of the new white paper that provides insight into the general requirements in a microbiological and physical testing program. In it, he discusses how combination products pose a unique set of challenges to package validation engineers.

Titled, “Get with the Program: Having a Solid Package Validation Program Can Prevent Failure of Combination Products,” the paper is available for download from: http://www.microtestlabs.com/packaging-validation-paper.

In the white paper, Richter discusses the challenges of packaging validation and some of the options for testing. He provides a summary of the standardized test methods commonly used in the U.S. for satisfying ANSI/AAMI/ISO 11607 requirements, and outlines the steps in the packaging validation process. He also focuses on the points to consider during packaging validation studies for cell therapy products.

“All device and combination product manufacturers are required to have a robust package validation program, and medical device stability package validation programs should be designed to encompass the overt product storage and shipment conditions,” Richter said. “The necessity to develop a robust packaging validation regimen cannot be overstated. A comprehensive regulatory approach to validation during early product development can save many weeks of redevelopment and testing activities.

“This white paper is presented to give medical device and combination product manufacturers a starting point for package validation programs,” he said.

Download the new, free white paper, Get with the Program: Having a Solid Package Validation Program Can Prevent Failure of Combination Products,” from: http://www.microtestlabs.com/packaging-validation-paper.

Steven Richter, Ph.D., is founder, president, and chief scientific officer of Microtest Laboratories, Inc., in Agawam, Mass. Dr. Richter founded Microtest in 1984 after a distinguished career at the U.S. Food & Drug Administration. Under his leadership, Microtest has provided the medical device, pharmaceutical, and biotechnology industries with premier testing and manufacturing support.

Follow Microtest Labs on Twitter @MicrotestLabs at http://twitter.com/MicrotestLabs.

About Microtest

Microtest is a leader in testing services and contract manufacturing for the medical device, pharmaceutical, and biotechnology industries. Based in Agawam, Massachusetts, U.S.A., the company’s expertise and flexible processes enhance product safety and security, accelerate time to market, and minimize supply chain disruption. For more information, visit http://www.microtestlabs.com or call 1-413-786-1680 or toll-free 1-800-631-1680.

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Public Relations contact, Boston:  Don Goncalves, dgoncalves@tizinc.com, 781-793-9380, for Tiziani Whitmyre Inc., http://www.tizinc.com/public-relations


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